TLE1[gene] and "single gene"[properties] - ClinVar

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Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2223361	NM_005077.5(TLE1):c.2186A>G (p.Tyr729Cys)	TLE1 (Y714C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518576	NM_005077.5(TLE1):c.2017G>A (p.Ala673Thr)	TLE1 (A683T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177796	NM_005077.5(TLE1):c.2011T>C (p.Trp671Arg)	TLE1 (W681R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378678	NM_005077.5(TLE1):c.2005G>A (p.Gly669Arg)	TLE1 (G654R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479139	NM_005077.5(TLE1):c.1962C>G (p.His654Gln)	TLE1 (H639Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457056	NM_005077.5(TLE1):c.1936C>T (p.Arg646Cys)	TLE1 (R656C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332839	NM_005077.5(TLE1):c.1913A>G (p.Asn638Ser)	TLE1 (N638S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514553	NM_005077.5(TLE1):c.1820C>T (p.Thr607Ile)	TLE1 (T592I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210640	NM_005077.5(TLE1):c.1668T>G (p.Ile556Met)	TLE1 (I541M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 625146	NM_005077.5(TLE1):c.1621G>A (p.Asp541Asn)	TLE1 (D526N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2311929	NM_005077.5(TLE1):c.1259G>A (p.Gly420Glu)	TLE1 (G430E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407209	NM_005077.5(TLE1):c.1244G>A (p.Arg415His)	TLE1 (R400H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410520	NM_005077.5(TLE1):c.1219G>A (p.Ala407Thr)	TLE1 (A392T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509590	NM_005077.5(TLE1):c.1207G>A (p.Ala403Thr)	TLE1 (A388T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293504	NM_005077.5(TLE1):c.1189A>G (p.Met397Val)	TLE1 (M407V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542227	NM_005077.5(TLE1):c.1185C>A (p.His395Gln)	TLE1 (H380Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382838	NM_005077.5(TLE1):c.1165G>A (p.Ala389Thr)	TLE1 (A374T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222631	NM_005077.5(TLE1):c.1081C>T (p.Pro361Ser)	TLE1 (P371S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177798	NM_005077.5(TLE1):c.956C>T (p.Thr319Ile)	TLE1 (T329I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326283	NM_005077.5(TLE1):c.935C>T (p.Thr312Met)	TLE1 (T322M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623556	NM_005077.5(TLE1):c.887C>T (p.Ser296Phe)	TLE1 (S296F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326281	NM_005077.5(TLE1):c.820G>A (p.Asp274Asn)	TLE1 (D284N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347233	NM_005077.5(TLE1):c.779C>T (p.Pro260Leu)	TLE1 (P260L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455375	NM_005077.5(TLE1):c.773C>T (p.Ser258Phe)	TLE1 (S258F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177797	NM_005077.5(TLE1):c.640C>T (p.Arg214Cys)	TLE1 (R214C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326285	NM_005077.5(TLE1):c.584A>G (p.Glu195Gly)	TLE1 (E195G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292774	NM_005077.5(TLE1):c.517G>A (p.Gly173Arg)	TLE1 (G183R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412551	NM_005077.5(TLE1):c.497C>T (p.Ala166Val)	TLE1 (A176V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326280	NM_005077.5(TLE1):c.424C>T (p.Pro142Ser)	TLE1 (P152S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326286	NM_005077.5(TLE1):c.318G>C (p.Gln106His)	TLE1 (Q106H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546848	NM_005077.5(TLE1):c.155G>A (p.Ser52Asn)	TLE1 (S52N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 775274	NM_005077.5(TLE1):c.63T>C (p.Thr21=)	TLE1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3326282	NM_005077.5(TLE1):c.52T>C (p.Phe18Leu)	TLE1 (F18L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216295	NM_005077.5(TLE1):c.48G>T (p.Gln16His)	TLE1 (Q16H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326287	NM_005077.5(TLE1):c.38C>T (p.Ala13Val)	TLE1 (A13V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488487	NM_005077.5(TLE1):c.22C>T (p.Pro8Ser)	TLE1 (P8S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1340424	GRCh37/hg19 9q21.31-21.32(chr9:83887235-84226416)x3	TLE1	Copy number gain	not provided	GUncertain significance
Select item 979265	GRCh37/hg19 9q21.31-21.32(chr9:83875106-84219691)x3	TLE1	Copy number gain	not provided	GUncertain significance

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Items: 38